Variants studied for hyperplastic polyposis syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
4	4	178	2	1	188

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
RNF43	4	4	178	2	1	188

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Baylor Genetics	0	0	155	0	0	155
Fulgent Genetics, Fulgent Genetics	0	0	31	2	0	33
OMIM	2	0	0	0	0	2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	2	0	0	0	2
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas	0	0	2	0	0	2
MVZ Medizinische Genetik Mainz	2	0	0	0	0	2
Institute of Human Genetics, University of Goettingen	0	1	0	0	0	1
Revvity Omics, Revvity	0	0	1	0	0	1
The Canberra Hospital	1	0	0	0	0	1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India	0	1	0	0	0	1
Genome-Nilou Lab	0	0	0	0	1	1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	0	1	0	0	1

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